Cypress Medical recalls 60mL syringes (Catalog 869662) that were inadvertently shipped without FDA clearance due to an internal order error. No action needed as they are on quarantine.
The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
Cypress Medical is recalling 60mL syringes with catalog number 869662 that were shipped without FDA clearance. These syringes are on quarantine and no action is required as they were inadvertently shipped due to an internal order processing error.
The syringes were inadvertently shipped without FDA clearance due to an internal order processing error. They are currently on quarantine, meaning they are not being distributed to customers.
Healthcare professionals and medical facilities that may have received these syringes. The risk is low as the syringes are on quarantine and no action is needed.
Check for catalog number 869662 on the syringe packaging. These syringes were shipped by Cypress Medical under the McKesson brand.
Look for catalog number 869662 on the syringe packaging or label.
No, the syringes are on quarantine and no action is needed as they were inadvertently shipped due to an internal order processing error.
The syringes were inadvertently shipped without FDA clearance due to an internal order processing error, so they are on quarantine.
No action is required as the syringes are on quarantine and were inadvertently shipped due to an internal order processing error.
We’ve drafted a message you can send Cypress Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-3154-2024 — Cypress Medical Cypress Medical Hello, I own a Cypress Medical that is covered by recall Z-3154-2024 from Cypress Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
